What is Scale-Up and Post Approval Changes (SUPAC) report?
The Scale-Up and Post-Approval Changes (SUPAC) report refers to a set of FDA guidelines that provide recommendations for pharmaceutical manufacturers on how to handle changes... Read More
Sign In
|Sign Up
Please sign in first
Not a member?
Please simply create an account before buying/booking any courses.
Create an account for free!
Blog
What is clinically significant endpoint?
A clinically significant endpoint is an outcome or event in a clinical trial that provides a direct measure of the benefit or harm of a... Read More
The Uniqueness of Life Science Regulatory Affairs Course by Royed Training
In the fast-paced and highly regulated life science industry, professionals skilled in navigating the complexities of Regulatory Affairs (RA) are in high demand. Whether it’s... Read More
What is Real World Evidence in Pharma?
Real World Evidence (RWE) in the pharmaceutical industry refers to clinical evidence derived from the analysis of Real World Data (RWD), which captures how drugs,... Read More
Royed Training has been recognized as one of Silicon India’s Top 10 Most Promising Corporate Online Learning Providers!
Posted on24 Sep 2024
Comments0
[Kolkata, 24th of January, 2024] —We are proud to announce that Royed Training has been recognized as one of Silicon India’s Top 10 Most Promising... Read More
Unveiling the Variances: Medical Affairs and Market Access
Posted on27 Aug 2024
TagsMarket Access, Market Access meaning in Pharma, medical affairs, medical writing, pharma market access
Comments0
Market access and medical affairs are both crucial functions in the pharmaceutical domain, but they serve different purposes and involve distinct activities. Market Access Objective... Read More
What is MLR review?
MLR review is a comprehensive, multi-disciplinary process designed to ensure that all promotional and non-promotional materials related to pharmaceuticals, medical devices, and other healthcare products... Read More
What is WHO Prequalification (WHO PO) Status?
It is a quality assurance process managed by the World Health Organization (WHO) that assesses the quality, safety, and efficacy of medical products, including medicines,... Read More
Is bioburden and microbial limit test are same?
Bioburden and microbial limit tests are related but distinct tests used in microbiological quality control, especially in the pharmaceutical, medical device, and food industries. Here’s... Read More
Case Study – Mankind acquires Bharat Serums and Vaccines (BSV)
Posted on26 Jul 2024
Comments0
In July 2024, Mankind Pharma Limited announced a definitive agreement to acquire a 100% stake in Bharat Serums and Vaccines (BSV) Limited from Advent International... Read More
Protected: Demo Access – Biopharma Business Development
Posted on16 Jul 2024
Comments0
There is no excerpt because this is a protected post.
What is ECOWAS region?
The Economic Community of West African States (ECOWAS) is a regional political and economic union of countries located in West Africa. ECOWAS was established on... Read More